POSITION OBJECTIVE
Working under general supervision, the Research Assistant 2 is responsible for emotionally intelligent, culturally responsive, recruitment and collection of data for a large research project focused on patients with advanced cancer and their informal caregivers in accordance with an IRB-approved research protocol at University Hospitals Seidman Cancer Center main campus, and community locations and potentially other hospitals in the Cleveland area. The research assistant will provide input on overall study direction, addressing key data collection issues. In collaboration with the research team, this position will screen electronic medical records to determine subject eligibility, meet with patients and their caregivers to discuss the study and obtain consent and study data. The research assistant will communicate with clinical staff at the data collection site, assure human subjects’ compliance, and address problems that may occur. The research assistant may also work on other research projects related to the current cancer study.
ESSENTIAL FUNCTIONS
NONESSENTIAL FUNCTIONS
CONTACTS
Department: Daily contact with the principal investigator, co-investigators, project manager and other research team members to discuss research and maintain workflow. Contact with the other School of Nursing research staff and faculty conducting related studies.
University: Occasional contact with investigators conducting similar research within the university at education and research meetings.
External: Frequent contact with medical, nursing and medical records staff at University Hospitals of Cleveland Medical Center (main campus and satellite locations) to exchange information.
Students: Regular contact with BSN, MSN, DNP, PhD and other students who may assist with the study.
SUPERVISORY RESPONSIBILITY
This position has no direct supervision of staff employees. Train new staff; direct the work of students.
QUALIFICATIONS
Education/Experience/Licensing: Bachelor’s degree and 1 to 3 years of research, research assistance, or research related experience involving human participants; or Associate’s degree in an approved biotechnology program and 2 to 4 years of experience required. Experience and skill in interviewing patients and experience obtaining informed consent is desirable. Must be certified for the protection of human subjects within 30 days of hiring. Valid Ohio driver's license is preferred.
REQUIRED SKILLS
WORKING CONDITIONS
No exposure to hazardous materials. Must have reliable form of transportation for travel to study. Must be able to be on feet walking several hours a day between various hospital sites. This position is not eligible for remote work. This position will require an on-campus presence. Must be available Monday through Friday generally from the hours of 8:30 a.m. to 5:00 p.m. for participant data collection.
In employment, as in education, Case Western Reserve University is committed to Equal Opportunity and Diversity. Women, veterans, members of underrepresented minority groups, and individuals with disabilities are encouraged to apply.
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Case Western Reserve University provides reasonable accommodations to applicants with disabilities. Applicants requiring a reasonable accommodation for any part of the application and hiring process should contact the Office of Equity at 216-368-3066 to request a reasonable accommodation. Determinations as to granting reasonable accommodations for any applicant will be made on a case-by-case basis.
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